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rs587777852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777852(C;C)
Make rs587777852(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position142465860
GeneATR
is asnp
is mentioned by
dbSNPrs587777852
ebirs587777852
HLIrs587777852
Exacrs587777852
Varsomers587777852
Maprs587777852
PheGenIrs587777852
hapmaprs587777852
1000 genomesrs587777852
hgdprs587777852
ensemblrs587777852
gopubmedrs587777852
geneviewrs587777852
scholarrs587777852
googlers587777852
pharmgkbrs587777852
gwascentralrs587777852
openSNPrs587777852
23andMers587777852
23andMe allrs587777852
SNP Nexus

SNPshotrs587777852
SNPdbers587777852
MSV3drs587777852
GWAS Ctlgrs587777852
Max Magnitude0
ClinVar
Risk rs587777852(C;C)
Alt rs587777852(C;C)
Reference rs587777852(G;G)
Significance Pathogenic
Disease Seckel syndrome 1
Variation info
Gene ATR
CLNDBN Seckel syndrome 1
Reversed 0
HGVS NC_000003.11:g.142184702G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144693.3,